Women, Tibetan -- India -- New Delhi : Angu, une femme sur le fil(m) / un film de Fabienne le Houerou ; producteurs, Cultura Mundi, CNRS-IREMAM, MMSH-LabexMed
New Democratic Party of Manitoba. / http://id.loc.gov/authorities/names/n83025286 : Disengaged? : fixed date, democracy, and understanding the 2011 Manitoba election / [edited by] Andrea D. Rounce and Jared J. Wesley
New Development Bank. / http://id.loc.gov/authorities/names/nb2015008932 : Making sustainable development the key focus of the BRICS New Development Bank / Talitha Bertelsmann-Scott, Canelle Friis & Cyril Prinsloo
Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
Process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to FDA
Here are entered works on the medieval movement initiated by Gerard Groote, which resulted in the founding of the Brothers of the Common Life and the Windesheim Congregation of Augustinian Canons
New directions in the law of the sea. New series -- Indexes : New directions in the law of the sea. Reference and finding tools. New series / compiled and edited by Kenneth R. Simmonds with the collaboration of specialist consulting editors
Process that is gone through in order for a drug to receive approval by a government regulatory agency. This includes any required pre-clinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance of the drug